Wednesday Oct 5, 2016
8:00 AM - 5:00 PM EDT
October 5, 2016
8:00am to 5:00pm
Capstone Center
850 Oval Drive
Raleigh, NC 27695
$100
This course presents the regulatory requirements and best practices for pharmaceutical documents, documentation, and record keeping. Topics covered will include: a review of the differences between documents and records; the typical ISO 9001 document hierarchy as well as an explanation and appropriate content of each document level; record keeping requirements including the electronic signature and record keeping requirements of 21 CFR Part 11; and the appropriateness and qualification of Excel spreadsheets for record keeping. General good documentation practices incorporating the requirements detailed in FDA's Guidance to Industry "“Data Integrity and Compliance With cGMP” are also reviewed.
Printed courtesy of www.nclifesci.org/ – Contact the NC Life Sciences Organization for more information.
4505 Emperor Blvd, Ste 105, Durham, NC 27703 – (919) 281-8960 – Admin@NCLifeSci.org